Synthesis of 4-styrylquinazolines enabled by a hypervalent iodine-promoted oxidative amination cascade
Year: 2025
Type: article
Abstract: Efficient synthetic routes to pharmaceutically important 4-styrylquinazolines scaffolds are of considerable interest. Herein, we report a concise synthesis of 4-styrylquinazoline derivatives via a hypervalent iodine-promoted oxidative amination cascade. Readily available N -(2-acetophenyl)acetamides and benzylamines are employed, with the latter acting as both carbon and nitrogen donors, enabling simultaneous formation of the quinazoline core and the exocyclic alkene. This operationally simple and atom-economical strategy provides a streamlined alternative to conventional stepwise approaches.
Source: Tetrahedron Chem
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $2,660
OpenAlex ID: W4417013618
